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dc.contributor.authorVikberg Wernström, Joel
dc.contributor.authorGasiorowski, Ludwik
dc.contributor.authorHejnol, Andreas Helmut
dc.date.accessioned2022-11-28T08:53:42Z
dc.date.available2022-11-28T08:53:42Z
dc.date.issued2022-08-19
dc.description.abstract<p><b> Background</b> Brachiopods and molluscs are lophotrochozoans with hard external shells which are often believed to have evolved convergently. While palaeontological data indicate that both groups are descended from biomineralising Cambrian ancestors, the closest relatives of brachiopods, phoronids and bryozoans, are mineralised to a much lower extent and are comparatively poorly represented in the Palaeozoic fossil record. Although brachiopod and mollusc shells are structurally analogous, genomic and proteomic evidence indicates that their formation involves a complement of conserved, orthologous genes. Here, we study a set of genes comprised of 3 homeodomain transcription factors, one signalling molecule and 6 structural proteins which are implicated in mollusc and brachiopod shell formation, search for their orthologs in transcriptomes or genomes of brachiopods, phoronids and bryozoans, and present expression patterns of 8 of the genes in postmetamorphic juveniles of the rhynchonelliform brachiopod <i>T. transversa</i>. <p><b> Results</b> Transcriptome and genome searches for the 10 target genes in the brachiopods <i>Terebratalia transversa, Lingula anatina, Novocrania anomala</i>, the bryozoans <i>Bugula neritina and Membranipora membranacea</i>, and the phoronids <i>Phoronis australis and Phoronopsis harmeri</i> resulted in the recovery of orthologs of the majority of the genes in all taxa. While the full complement of genes was present in all brachiopods with a single exception in <i>L. anatina</i>, a bloc of four genes could consistently not be retrieved from bryozoans and phoronids. The genes <i>engrailed, distal-less, ferritin, perlucin, sp1 and sp2</i> were shown to be expressed in the biomineralising mantle margin of <i>T. transversa</i> juveniles. <p><b> Conclusions</b> The gene expression patterns we recovered indicate that while mineralised shells in brachiopods and molluscs are structurally analogous, their formation builds on a homologous process that involves a conserved complement of orthologous genes. Losses of some of the genes related to biomineralisation in bryozoans and phoronids indicate that loss of the capacity to form mineralised structures occurred already in the phoronid–bryozoan stem group and supports the idea that mineralised skeletons evolved secondarily in some of the bryozoan subclades.en_US
dc.description.sponsorshipEUen_US
dc.identifier.citationVikberg Wernström, Gasiorowski, Hejnol. Brachiopod and mollusc biomineralisation is a conserved process that was lost in the phoronid–bryozoan stem lineage. EVODEVO. 2022;13:17:1-11en_US
dc.identifier.cristinIDFRIDAID 2053225
dc.identifier.doi10.1186/s13227-022-00202-8
dc.identifier.issn2041-9139
dc.identifier.urihttps://hdl.handle.net/10037/27557
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.journalEVODEVO
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/648861/EU/The evolution of mesoderm and its differentiation into cell types and organ systems/EVOMESODERM/en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.subjectVDP::Matematikk og naturvitenskap: 400::Zoologiske og botaniske fag: 480::Marinbiologi: 497en_US
dc.subjectVDP::Mathematics and natural scienses: 400::Zoology and botany: 480::Marine biology: 497en_US
dc.subjectVDP::Matematikk og naturvitenskap: 400::Basale biofag: 470::Molekylærbiologi: 473en_US
dc.subjectVDP::Mathematics and natural scienses: 400::Basic biosciences: 470::Molecular biology: 473en_US
dc.titleBrachiopod and mollusc biomineralisation is a conserved process that was lost in the phoronid–bryozoan stem lineageen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)